Canonical Allele Identifier: CA422373951
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649876C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680744C>G , CM000663.2:g.186680744C>G GRCh38
NC_000001.10:g.186649876C>G , CM000663.1:g.186649876C>G GRCh37
NC_000001.9:g.184916499C>G NCBI36
NG_028206.2:g.4684G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-154G>C (PTGS2) ENSP00000506242.1:n.-154G>C
NR_125801.1:n.91C>G (PACERR)
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